WO2011055493A1 - Novel fluorenylamine compound, organic light emitting device containing the same, material for organic light emitting device, display apparatus, and image input apparatus - Google Patents
Novel fluorenylamine compound, organic light emitting device containing the same, material for organic light emitting device, display apparatus, and image input apparatus Download PDFInfo
- Publication number
- WO2011055493A1 WO2011055493A1 PCT/JP2010/006153 JP2010006153W WO2011055493A1 WO 2011055493 A1 WO2011055493 A1 WO 2011055493A1 JP 2010006153 W JP2010006153 W JP 2010006153W WO 2011055493 A1 WO2011055493 A1 WO 2011055493A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- light emitting
- emitting device
- organic light
- compound
- fluorenylamine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 91
- 239000000463 material Substances 0.000 title claims description 47
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims abstract description 7
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 7
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 7
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 7
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims abstract description 7
- 230000005525 hole transport Effects 0.000 claims description 20
- 150000002894 organic compounds Chemical class 0.000 claims description 17
- 239000010410 layer Substances 0.000 description 65
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 18
- 239000010408 film Substances 0.000 description 15
- 239000000243 solution Substances 0.000 description 15
- 239000000758 substrate Substances 0.000 description 9
- -1 as a main structure Chemical class 0.000 description 8
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 description 7
- 239000010409 thin film Substances 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229940125904 compound 1 Drugs 0.000 description 5
- 238000000151 deposition Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229940027991 antiseptic and disinfectant quinoline derivative Drugs 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 150000002220 fluorenes Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 229920000123 polythiophene Polymers 0.000 description 3
- 150000003252 quinoxalines Chemical class 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- 238000004528 spin coating Methods 0.000 description 3
- 238000001771 vacuum deposition Methods 0.000 description 3
- WTAPZWXVSZMMDG-UHFFFAOYSA-N 1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].C=1C=CC=CC=1C=CC(=O)C=CC1=CC=CC=C1 WTAPZWXVSZMMDG-UHFFFAOYSA-N 0.000 description 2
- 229910001148 Al-Li alloy Inorganic materials 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 150000001454 anthracenes Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001716 carbazoles Chemical class 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 229920001940 conductive polymer Polymers 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000001989 lithium alloy Substances 0.000 description 2
- AFRJJFRNGGLMDW-UHFFFAOYSA-N lithium amide Chemical compound [Li+].[NH2-] AFRJJFRNGGLMDW-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 150000002790 naphthalenes Chemical class 0.000 description 2
- 229920000767 polyaniline Polymers 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 150000003220 pyrenes Chemical class 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000005259 triarylamine group Chemical group 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 1
- NJJDBOFDNCZGSP-UHFFFAOYSA-N 3-bromo-9h-fluorene Chemical compound C1=CC=C2C3=CC(Br)=CC=C3CC2=C1 NJJDBOFDNCZGSP-UHFFFAOYSA-N 0.000 description 1
- CYYNGFHAPUXXMH-UHFFFAOYSA-N CC(C)(C)c(cc1cc2)cc3c1c1c2c(-c(cc2)cc(C(C)(C)c4c5)c2-c4ccc5-c(cc2)cc4c2-c2ccccc2C4(C)C)ccc1cc3 Chemical compound CC(C)(C)c(cc1cc2)cc3c1c1c2c(-c(cc2)cc(C(C)(C)c4c5)c2-c4ccc5-c(cc2)cc4c2-c2ccccc2C4(C)C)ccc1cc3 CYYNGFHAPUXXMH-UHFFFAOYSA-N 0.000 description 1
- 0 CC1(C)c(cc(cc2)-c3ccc-4c5*3cccc5-c3ccccc-43)c2-c(cc2)c1cc2-c(cc1)c2c3c1-c1ccccc1-c3ccc2 Chemical compound CC1(C)c(cc(cc2)-c3ccc-4c5*3cccc5-c3ccccc-43)c2-c(cc2)c1cc2-c(cc1)c2c3c1-c1ccccc1-c3ccc2 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920000265 Polyparaphenylene Chemical class 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000012905 input function Methods 0.000 description 1
- 150000002503 iridium Chemical class 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000001840 matrix-assisted laser desorption--ionisation time-of-flight mass spectrometry Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 150000007978 oxazole derivatives Chemical class 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- 150000005041 phenanthrolines Chemical class 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 150000004033 porphyrin derivatives Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 150000003216 pyrazines Chemical class 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000010944 silver (metal) Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 238000001269 time-of-flight mass spectrometry Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000001651 triphenylamine derivatives Chemical class 0.000 description 1
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
- C07C211/61—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton with at least one of the condensed ring systems formed by three or more rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/18—Fluorenes; Hydrogenated fluorenes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/10—Triplet emission
Definitions
- the present invention relates to a novel fluorenylamine compound, a material for an organic light emitting device, an organic light emitting device containing such a novel fluorenylamine compound, a display apparatus including such an organic light emitting device, and an image input apparatus including such an organic light emitting device.
- An organic light emitting device includes a positive electrode, a negative electrode, and an organic compound layer disposed between the positive electrode and the negative electrode.
- An organic compound used for such an organic light emitting device is required to have thermal stability. This is because functions of the organic compound are degraded by heat.
- Patent Literature 1 describes, as a compound having a high thermal stability, a compound illustrated as Compound 1 below.
- Compound 1 which is a compound described in Patent Literature 1, does not have a sufficiently large band gap and does not have a sufficiently high lowest excited triplet level.
- the present invention provides an organic compound that has a high thermal stability, a large band gap, and a high lowest excited triplet level.
- the present invention provides a fluorenylamine compound represented by a general formula below,
- R 1 to R 6 are each independently selected from a hydrogen atom and alkyl groups; R 21 to R 23 are each independently selected from a hydrogen atom and the alkyl groups.
- the alkyl groups are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group.
- the present invention can provide an organic compound that has a high glass transition temperature.
- this organic compound includes three fluorenyl groups bonded to a nitrogen atom at the 3-positions, and hence has a large band gap and a high lowest excited triplet level.
- Fig. 1 is a schematic sectional view illustrating organic light emitting devices and thin-film transistor (TFT) devices connected to the organic light emitting devices.
- TFT thin-film transistor
- the present invention provides a novel fluorenylamine compound represented by the following general formula.
- R 1 to R 6 are each independently selected from a hydrogen atom and alkyl groups.
- R 21 to R 23 are each independently selected from a hydrogen atom and the alkyl groups.
- the alkyl groups are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group.
- a fluorenylamine compound according to the present invention is a compound including, as a main structure, a nitrogen atom and three fluorenyl groups bonded to the nitrogen atom at the 3-positions.
- R 1 to R 6 which are bonded to the main structure in the general formula, are each independently selected from a hydrogen atom and alkyl groups.
- R 21 to R 23 which are also bonded to the main structure in the general formula, are each independently selected from a hydrogen atom and alkyl groups.
- alkyl groups that may be included in R 1 to R 6 and R 21 to R 23 include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group.
- This low ionization potential means that positive holes are readily injected from a positive electrode, which leads to the operation of an organic light emitting device at a low voltage.
- the low ionization potential means that the ionization potential is close to the vacuum level.
- a fluorenylamine compound according to the present invention has a high glass transition temperature (Tg) and a high thermal stability. This is because all the three fluorenyl groups are bonded at the 3-positions.
- the fluorenylamine compound includes three fluorenyl groups that are all bonded to a nitrogen atom at the 3-positions, compared with Compound 1 including fluorenyl groups that are bonded to a nitrogen atom at the 2-positions, the fluorenylamine compound has a low flatness in its entirety and a low probability of association between molecules. Thus, the fluorenylamine compound forms a stable amorphous film in which crystallization is less likely to occur.
- a fluorenylamine compound according to the present invention since all the three fluorenyl groups are bonded to a nitrogen atom at the 3-positions, conjugation is not achieved in the entirety of the fluorene molecules but is locally achieved in portions where the fluorenyl groups are bonded to the nitrogen atom and near the portions. As a result, the fluorenylamine compound has a large band gap and a high lowest excited triplet level (T1). Table 1 below summarizes T1s measured in a toluene solution at -78degree(Celsius).
- Exemplified compound A1 Compared with the T1 of Compound 1, since the T1 of Exemplified compound A1 has a large difference from the T1 of Ir(ppy)3, which is a green phosphorescence emitting material, triplet excitons are less likely to move from a light emitting layer to a hole transport layer, which is adjacent to the light emitting layer. In contrast, since the T1 of Compound 1 is almost the same as that of the green phosphorescence emitting material, some triplet excitons probably move from a light emitting layer to a hole transport layer, which is adjacent to the light emitting layer. Thus, Exemplified compound A1 can be suitably used as a host material of a hole transport layer or a light emitting layer in a device containing the green phosphorescence emitting material.
- a phosphorescence emitting material is a compound that emits phosphorescence at room temperature.
- a fluorescence emitting material is a compound that emits fluorescence at room temperature.
- a compound having the largest weight proportion is a host material and compounds having smaller weight proportions than the host material are guest materials.
- a fluorenylamine compound according to the present invention is also suitably used as a host material in a light emitting device including a light emitting layer containing the host material and a guest material. Since a fluorenylamine compound according to the present invention has a large band gap, such a fluorenylamine compound can be used as the host material of a light emitting layer containing a blue fluorescence emitting material requiring a large band gap. Thus, excitons generated in the host material can be moved to the guest material and the light can be efficiently emitted. Furthermore, a fluorenylamine compound according to the present invention may be used as the host material of a light emitting layer of an organic light emitting device containing a fluorescence emitting material that emits green light or red light.
- a fluorenylamine compound according to the present invention has a high T1
- the fluorenylamine compound can be suitably used as the host material of a light emitting layer containing a green fluorescence emitting material. This is because the fluorenylamine compound has a higher T1 than the green fluorescence emitting material. Accordingly, triplet excitons generated in the host material can be moved to the guest material and the light can be efficiently emitted.
- a fluorescence emitting material a green fluorescence emitting material or a red fluorescence emitting material may be used.
- An organic light emitting device includes a pair of electrodes and an organic compound layer disposed between the pair of electrodes.
- the pair of electrodes are electrodes that have polarities opposite to each other, for example, a positive electrode and a negative electrode.
- An electric field in a forward direction in which the organic light emitting device emits light may be applied to the pair of electrodes.
- an electric field in a backward direction that is opposite to the forward direction may be applied to the pair of electrodes.
- the organic compound layer may be a single layer or a multilayer.
- the organic compound layer contains a fluorenylamine compound according to the present invention.
- the multilayer may include layers appropriately selected from a hole injection layer, a hole transport layer, a light emitting layer, a hole and exciton blocking layer, an electron transport layer, an electron injection layer, and the like.
- a fluorenylamine compound according to the present invention includes an arylamine
- the fluorenylamine compound is excellent in terms of hole transport and is suitably provided in a light emitting layer or a hole transport layer disposed between a light emitting layer and a positive electrode in an organic light emitting device.
- a hole transport layer does not contain a fluorenylamine compound according to the present invention
- a compound contained in the hole transport layer include, but are not limited to, triarylamine derivatives, phenylenediamine derivatives, stilbene derivatives, phthalocyanine derivatives, porphyrin derivatives, poly(vinylcarbazole), poly(thiophene), and other conductive polymers.
- examples of the host material of the light emitting layer include, but are not limited to, condensed ring compounds (for example, fluorene derivatives, naphthalene derivatives, anthracene derivatives, pyrene derivatives, carbazole derivatives, quinoxaline derivatives, and quinoline derivatives); organic aluminum complexes such as tris(8-quinolinolate)aluminum; organic zinc complexes; triphenylamine derivatives; and polymer derivatives such as poly(fluorene) derivatives and poly(phenylene) derivatives.
- condensed ring compounds for example, fluorene derivatives, naphthalene derivatives, anthracene derivatives, pyrene derivatives, carbazole derivatives, quinoxaline derivatives, and quinoline derivatives
- organic aluminum complexes such as tris(8-quinolinolate)aluminum
- organic zinc complexes organic zinc complexes
- triphenylamine derivatives triphenylamine
- a fluorenylamine compound according to the present invention is the host material of a light emitting layer
- examples of a guest material of the light emitting layer include, but are not limited to, condensed ring compounds (for example, fluorene derivatives, naphthalene derivatives, anthracene derivatives, pyrene derivatives, carbazole derivatives, quinoxaline derivatives, and quinoline derivatives); compounds in which such condensed ring compounds have been substituted with substituents such as amino groups; iridium complexes; and platinum complexes.
- Examples of a compound for forming a hole injection layer disposed between a positive electrode and a hole transport layer include compounds such as copper phthalocyanine, triarylamine derivatives, fluorocarbon polymers, polyaniline, and polythiophene.
- a fluorenylamine compound according to the present invention may be contained in both a hole transport layer and a light emitting layer of a single organic light emitting device.
- Examples of a compound for forming an electron injection layer or an electron transport layer that is disposed between a light emitting layer and a negative electrode include, but are not limited to, oxadiazole derivatives, oxazole derivatives, pyrazine derivatives, triazole derivatives, triazine derivatives, quinoline derivatives, quinoxaline derivatives, phenanthroline derivatives, and organic aluminum complexes.
- a material used for forming a positive electrode has a high work function.
- a material include, but are not limited to, elemental metals such as Au, Pt, Ag, Cu, Ni, Pd, Co, Se, V, and W; alloys of such metals; metal oxides such as ITO and IZO; and conductive polymers such as polyaniline, polypyrrole, and polythiophene. These electrode materials may be used alone or in combination.
- a positive electrode may have a single layer configuration or a multilayer configuration.
- a material used for forming a negative electrode has a low work function.
- examples of such a material include, but are not limited to, alkali metals such as Li; alkaline-earth metals such as Ca; elemental metals such as Al, Ti, Mn, Ag, Pb, and Cr; alloys of such elemental metals; and metal oxides such as ITO.
- an organic compound layer may be formed by, for example, the following method.
- the layer may be formed by vacuum deposition or by a solution application method in which a material is dissolved in an appropriate solvent, the resultant solution is applied to a predetermined position, and the applied solution is dried to remove the solvent.
- An organic light emitting device may be used for a display apparatus or a lighting apparatus.
- such an organic light emitting device may be used for, for example, an exposure light source of an image forming apparatus employing an electrophotographic technique or a backlight of a liquid crystal display apparatus.
- a display apparatus includes an organic light emitting device according to the present invention in a display section.
- the display section includes a plurality of pixels.
- Such a pixel includes an organic light emitting device according to the present invention and a TFT device.
- the positive electrode or the negative electrode of the organic light emitting device is connected to the drain electrode or the source electrode of the TFT device.
- Such a display apparatus may be used as an image display apparatus for a PC or the like.
- such a display apparatus may be used for a display section of an image pickup apparatus such as a digital camera or a digital video camera.
- an image pickup apparatus includes a display section and an image pickup section including an image pickup system such as a lens for picking up images.
- Such a display apparatus may be used not only for a display section of an image pickup apparatus but also for a display section of an inkjet printer.
- Such a display apparatus may be an image input apparatus including an image input section configured to receive data from an area CCD, a linear CCD, a memory card, or the like.
- Such a display apparatus may serve as a display section and an operation panel of an image pickup apparatus or an inkjet printer. That is, the display apparatus may have an image output function of displaying images on the basis of image data input from the outside and an input function of receiving processing data for the images.
- Such a display apparatus may be used for a display section of a multifunction printer.
- Fig. 1 is a schematic sectional view illustrating an organic light emitting device according to the present invention and a TFT device serving as an example of a switching device that is configured to switch between the light-emitting state and non-light-emitting state of the organic light emitting device and is connected to the organic light emitting device.
- Fig. 1 illustrates two sets of the organic light emitting device and the TFT device. The structure of these devices will be described below in detail.
- the display apparatus in Fig. 1 includes a substrate 1 composed of glass or the like and a vapor barrier film 2 that is disposed on the substrate 1 and is configured to protect the TFT devices or an organic compound layer.
- the display apparatus also includes a gate electrode 3 formed of a metal, a gate insulation film 4, and a semiconductor layer 5.
- a TFT device 8 includes the semiconductor layer 5, a drain electrode 6, and a source electrode 7.
- An insulation film 9 is disposed over the TFT device 8.
- a positive electrode 11 of an organic EL device is connected to the source electrode 7 through a contact hole 10. Such a configuration is not limitative for a display apparatus and it will suffice that any one of the positive electrode and the negative electrode is connected to any one of the source electrode and the drain electrode of the TFT device.
- an organic compound layer 12 which is a multilayer organic compound layer, is illustrated as a single layer.
- a first protective layer 14 and a second protective layer 15 for suppressing degradation of the organic light emitting devices are disposed on a negative electrode 13.
- Use of a display apparatus including an organic light emitting device according to the present invention enables displaying of images with stability for a long period of time.
- Exemplified compound A1 represented by this formula was synthesized in the following manner.
- a 100 ml three-neck flask was prepared and charged with 0.40 g (1.46 mmol) of 3-bromofluorene, 0.35 g (14.6 mmol) of lithium amide (product name: lithium amide, manufactured by KISHIDA CHEMICAL Co., Ltd.), 0.49 g (5.0 mmol) of sodium tertiary butoxide (product name: sodium tertiary butoxide, manufactured by TOKYO CHEMICAL INDUSTRY CO., LTD.); further, 20 ml of xylene; while the solution was stirred at room temperature in a nitrogen atmosphere, 0.5 ml (0.15 mmol) of tri-tertiary-butylphosphine (10 wt% hexane solution); and then 0.67 mg (0.153 mmol) of palladium dibenzylideneacetone (product name: palladium dibenzylidene
- Exemplified compound A1 was subjected to 1 H-NMR measurement with an ECA-400 manufactured by JEOL Ltd. (solvent: deuterochloroform) and the delta values (ppm) thereof were found to be 7.56 (2H, dt), 7.42 (1H, dd), 7.32-7.25 (3H, m), 7.10 (1H, dd), and 1.52(6H, s).
- the band gap of Exemplified compound A1 was determined from an ultraviolet-visible light absorption spectrum and it was found to be 3.02 eV. In this specification, each band gap was determined with a spectrophotometer U-3010 manufactured by Hitachi, Ltd. from absorption ends of a thin film formed on a glass substrate.
- the ionization potential of Exemplified compound A1 was determined with an atmospheric photoelectron spectrometer (measurement apparatus name: AC-1, manufactured by Riken Keiki Co., Ltd.) and it was found to be 5.51 eV.
- Exemplified compound A1 was measured with a Pyris 1 (manufactured by PerkinElmer, Inc.) and it was found to be 154degree(Celsius). Thus, Exemplified compound A1 had a high thermal stability.
- Exemplified compound A1 was further evaluated in terms of amorphousness.
- a chloroform solution of Exemplified compound A1 was prepared such that the concentration of Exemplified compound A1 was 0.1 wt%. This solution was dropped onto a glass substrate and spin-coating was performed to form a thin film. After that, the thin film was dried with a vacuum oven at 80degree(Celsius) for 10 minutes to remove the solvent in the thin film.
- the resultant substrate was left in the oven at 60degree(Celsius) for a week. Then, the occurrence of crystallization in the film was visually inspected and it was confirmed that no crystallization occurred.
- An organic light emitting device according to the present invention was produced by the following method.
- ITO indium-tin oxide
- a positive electrode was formed.
- This positive electrode was subjected to ultrasonic washing with acetone and then isopropyl alcohol (IPA) and then to boiling washing with IPA, and then dried. Furthermore, the positive electrode was subjected to UV and ozone cleaning.
- IPA isopropyl alcohol
- a first hole transport layer was formed on the positive electrode in the following manner.
- a chloroform solution of Compound 3-1 illustrated below was prepared such that the concentration of Compound 3-1 was 0.1 wt%.
- This solution was dropped onto the ITO electrode and spin-coating was performed initially at 500 RPM for 10 seconds and then 1,000 RPM for a minute. After that, the applied solution was dried in a vacuum oven at 80degree(Celsius) for 10 minutes to remove the solvent in the thin film. Thus, the first hole transport layer having a thickness of 11 nm was formed.
- a second hole transport layer having a thickness of 20 nm was formed on the first hole transport layer by depositing Exemplified compound A1.
- film formation conditions used were a degree of vacuum of 1.0 * 10 -4 Pa and a film formation rate of 0.1 nm/sec.
- a light emitting layer having a thickness of 25 nm was then formed by codepositing Compound 3-3 (illustrated below) serving as a host material and Compound 3-2 (illustrated below) serving as a guest material such that the proportion of Compound 3-3 was 95 wt% and the proportion of Compound 3-2 was 5 wt%.
- An electron transport layer having a thickness of 20 nm was then formed by depositing Compound 3-4 illustrated below.
- a metal layer film having a thickness of 0.5 nm was then formed of a deposition material composed of an aluminum-lithium alloy (concentration of lithium: 1 atom%) on the light emitting layer by a vacuum deposition method.
- an aluminum film having a thickness of 150 nm was formed by a vacuum deposition method.
- an organic light emitting device including the aluminum-lithium alloy film serving as a negative electrode was formed.
- film formation conditions used were a degree of vacuum of 1.0 * 10 -4 Pa and a film formation rate of 1.0 to 1.2 nm/sec.
- the thus-formed device was subjected to performance evaluation with a spectroradiometer SR-3 (manufactured by TOPCON CORPORATION). As a result, a blue light emission having a light emission efficiency of 3.23 cd/A and a light emission wavelength of 474.6 nm was observed under the applied voltage of 4.0 V.
- An organic light emitting device in which a fluorenylamine compound according to the present invention was used as the host material of a light emitting layer was produced.
- a film was formed of ITO by a sputtering method so as to have a thickness of 120 nm on a glass substrate serving as a substrate to prepare a positive electrode.
- This positive electrode was subjected to ultrasonic washing with acetone and then isopropyl alcohol (IPA) and then to boiling washing with IPA, then dried, and then UV and ozone cleaning.
- IPA isopropyl alcohol
- a hole transport layer was formed on the positive electrode in the following manner.
- a chloroform solution of Compound 3-1 (illustrated above) was prepared such that the concentration of Compound 3-1 was 0.1 wt%.
- This solution was dropped onto the ITO electrode and spin-coating was performed initially at 500 RPM for 10 seconds and then 1,000 RPM for a minute. After that, the applied solution was dried in a vacuum oven at 80degree(Celsius) for 10 minutes to remove the solvent in the thin film. Thus, the hole transport layer was formed.
- a light emitting layer having a thickness of 25 nm was then formed by codepositing Exemplified compound A1 serving as a host material and Compound 3-2 (illustrated above) serving as a guest material such that the proportion of Exemplified compound A1 was 95 wt% and the proportion of Compound 3-2 was 5 wt%. Furthermore, an electron transport layer and an Al electrode were formed as in EXAMPLE 2.
- the thus-formed organic light emitting device was subjected to performance evaluation as in EXAMPLE 2. As a result, a good blue light emission having a light emission efficiency of 2.9 cd/A and a light emission wavelength of 475.0 nm was observed under the applied voltage of 4.0 V.
- the luminance of the device after a lapse of 100 hours was 81% of the initial luminance.
- each of R 1 to R 6 in the general formula is a methyl group was used.
- the methyl group is substituted with any one of a hydrogen atom, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group, similar advantages are provided.
- each of R 21 to R 23 in the general formula is a hydrogen atom was used.
- the hydrogen atom is substituted with any one of a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group, similar advantages are provided. This is because such a substituent enhances the degree of amorphousness of the compound without changing the electron state of the compound.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A novel fluorenylamine compound represented by a general formula below, where R1 to R6 are each independently selected from a hydrogen atom and alkyl groups; R21 to R23 are each independently selected from a hydrogen atom and the alkyl groups; and the alkyl groups are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group. [Chem. 2]
Description
The present invention relates to a novel fluorenylamine compound, a material for an organic light emitting device, an organic light emitting device containing such a novel fluorenylamine compound, a display apparatus including such an organic light emitting device, and an image input apparatus including such an organic light emitting device.
An organic light emitting device includes a positive electrode, a negative electrode, and an organic compound layer disposed between the positive electrode and the negative electrode.
An organic compound used for such an organic light emitting device is required to have thermal stability. This is because functions of the organic compound are degraded by heat.
Patent Literature 1 describes, as a compound having a high thermal stability, a compound illustrated as Compound 1 below.
Compound 1, which is a compound described in Patent Literature 1, does not have a sufficiently large band gap and does not have a sufficiently high lowest excited triplet level.
The present invention provides an organic compound that has a high thermal stability, a large band gap, and a high lowest excited triplet level.
Accordingly, the present invention provides a fluorenylamine compound represented by a general formula below,
In this general formula, R1 to R6 are each independently selected from a hydrogen atom and alkyl groups; R21 to R23 are each independently selected from a hydrogen atom and the alkyl groups.
The alkyl groups are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group.
The present invention can provide an organic compound that has a high glass transition temperature. In addition, this organic compound includes three fluorenyl groups bonded to a nitrogen atom at the 3-positions, and hence has a large band gap and a high lowest excited triplet level.
The present invention provides a novel fluorenylamine compound represented by the following general formula.
In this general formula, R1 to R6 are each independently selected from a hydrogen atom and alkyl groups. R21 to R23 are each independently selected from a hydrogen atom and the alkyl groups.
The alkyl groups are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group.
A fluorenylamine compound according to the present invention is a compound including, as a main structure, a nitrogen atom and three fluorenyl groups bonded to the nitrogen atom at the 3-positions. R1 to R6, which are bonded to the main structure in the general formula, are each independently selected from a hydrogen atom and alkyl groups. R21 to R23, which are also bonded to the main structure in the general formula, are each independently selected from a hydrogen atom and alkyl groups.
Examples of alkyl groups that may be included in R1 to R6 and R21 to R23 include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group.
Introduction of an alkyl group serving as a substituent into a fluorenyl group can decrease the ionization potential of the compound. This low ionization potential means that positive holes are readily injected from a positive electrode, which leads to the operation of an organic light emitting device at a low voltage. The low ionization potential means that the ionization potential is close to the vacuum level.
A fluorenylamine compound according to the present invention has a high glass transition temperature (Tg) and a high thermal stability. This is because all the three fluorenyl groups are bonded at the 3-positions.
Since the fluorenylamine compound includes three fluorenyl groups that are all bonded to a nitrogen atom at the 3-positions, compared with Compound 1 including fluorenyl groups that are bonded to a nitrogen atom at the 2-positions, the fluorenylamine compound has a low flatness in its entirety and a low probability of association between molecules. Thus, the fluorenylamine compound forms a stable amorphous film in which crystallization is less likely to occur.
In a fluorenylamine compound according to the present invention, since all the three fluorenyl groups are bonded to a nitrogen atom at the 3-positions, conjugation is not achieved in the entirety of the fluorene molecules but is locally achieved in portions where the fluorenyl groups are bonded to the nitrogen atom and near the portions. As a result, the fluorenylamine compound has a large band gap and a high lowest excited triplet level (T1). Table 1 below summarizes T1s measured in a toluene solution at -78degree(Celsius).
Compared with the T1 of Compound 1, since the T1 of Exemplified compound A1 has a large difference from the T1 of Ir(ppy)3, which is a green phosphorescence emitting material, triplet excitons are less likely to move from a light emitting layer to a hole transport layer, which is adjacent to the light emitting layer. In contrast, since the T1 of Compound 1 is almost the same as that of the green phosphorescence emitting material, some triplet excitons probably move from a light emitting layer to a hole transport layer, which is adjacent to the light emitting layer. Thus, Exemplified compound A1 can be suitably used as a host material of a hole transport layer or a light emitting layer in a device containing the green phosphorescence emitting material.
A phosphorescence emitting material is a compound that emits phosphorescence at room temperature. A fluorescence emitting material is a compound that emits fluorescence at room temperature.
Here, among compounds forming a light emitting layer, a compound having the largest weight proportion is a host material and compounds having smaller weight proportions than the host material are guest materials.
Due to the above-described advantage, when a compound according to the present invention is used for a hole transport layer, singlet excitons and triplet excitons generated in a light emitting layer are contained in the light emitting layer and hence the efficiency is enhanced.
A fluorenylamine compound according to the present invention is also suitably used as a host material in a light emitting device including a light emitting layer containing the host material and a guest material. Since a fluorenylamine compound according to the present invention has a large band gap, such a fluorenylamine compound can be used as the host material of a light emitting layer containing a blue fluorescence emitting material requiring a large band gap. Thus, excitons generated in the host material can be moved to the guest material and the light can be efficiently emitted. Furthermore, a fluorenylamine compound according to the present invention may be used as the host material of a light emitting layer of an organic light emitting device containing a fluorescence emitting material that emits green light or red light.
Since a fluorenylamine compound according to the present invention has a high T1, the fluorenylamine compound can be suitably used as the host material of a light emitting layer containing a green fluorescence emitting material. This is because the fluorenylamine compound has a higher T1 than the green fluorescence emitting material. Accordingly, triplet excitons generated in the host material can be moved to the guest material and the light can be efficiently emitted. As for such a fluorescence emitting material, a green fluorescence emitting material or a red fluorescence emitting material may be used.
Examples of a fluorenylamine compound according to the present invention will be illustrated below.
Hereinafter, an organic light emitting device according to the present invention will be described.
An organic light emitting device according to the present invention includes a pair of electrodes and an organic compound layer disposed between the pair of electrodes. The pair of electrodes are electrodes that have polarities opposite to each other, for example, a positive electrode and a negative electrode. An electric field in a forward direction in which the organic light emitting device emits light may be applied to the pair of electrodes. Alternatively, an electric field in a backward direction that is opposite to the forward direction may be applied to the pair of electrodes. The organic compound layer may be a single layer or a multilayer. The organic compound layer contains a fluorenylamine compound according to the present invention.
The multilayer may include layers appropriately selected from a hole injection layer, a hole transport layer, a light emitting layer, a hole and exciton blocking layer, an electron transport layer, an electron injection layer, and the like.
Since a fluorenylamine compound according to the present invention includes an arylamine, the fluorenylamine compound is excellent in terms of hole transport and is suitably provided in a light emitting layer or a hole transport layer disposed between a light emitting layer and a positive electrode in an organic light emitting device.
When a hole transport layer does not contain a fluorenylamine compound according to the present invention, for example, when a light emitting layer contains a fluorenylamine compound according to the present invention, examples of a compound contained in the hole transport layer include, but are not limited to, triarylamine derivatives, phenylenediamine derivatives, stilbene derivatives, phthalocyanine derivatives, porphyrin derivatives, poly(vinylcarbazole), poly(thiophene), and other conductive polymers.
When a light emitting layer does not contain a fluorenylamine compound according to the present invention, for example, when a hole transport layer contains a fluorenylamine compound according to the present invention, examples of the host material of the light emitting layer include, but are not limited to, condensed ring compounds (for example, fluorene derivatives, naphthalene derivatives, anthracene derivatives, pyrene derivatives, carbazole derivatives, quinoxaline derivatives, and quinoline derivatives); organic aluminum complexes such as tris(8-quinolinolate)aluminum; organic zinc complexes; triphenylamine derivatives; and polymer derivatives such as poly(fluorene) derivatives and poly(phenylene) derivatives.
When a fluorenylamine compound according to the present invention is the host material of a light emitting layer, examples of a guest material of the light emitting layer include, but are not limited to, condensed ring compounds (for example, fluorene derivatives, naphthalene derivatives, anthracene derivatives, pyrene derivatives, carbazole derivatives, quinoxaline derivatives, and quinoline derivatives); compounds in which such condensed ring compounds have been substituted with substituents such as amino groups; iridium complexes; and platinum complexes.
Examples of a compound for forming a hole injection layer disposed between a positive electrode and a hole transport layer include compounds such as copper phthalocyanine, triarylamine derivatives, fluorocarbon polymers, polyaniline, and polythiophene.
A fluorenylamine compound according to the present invention may be contained in both a hole transport layer and a light emitting layer of a single organic light emitting device.
Examples of a compound for forming an electron injection layer or an electron transport layer that is disposed between a light emitting layer and a negative electrode include, but are not limited to, oxadiazole derivatives, oxazole derivatives, pyrazine derivatives, triazole derivatives, triazine derivatives, quinoline derivatives, quinoxaline derivatives, phenanthroline derivatives, and organic aluminum complexes.
A material used for forming a positive electrode has a high work function. Examples of such a material include, but are not limited to, elemental metals such as Au, Pt, Ag, Cu, Ni, Pd, Co, Se, V, and W; alloys of such metals; metal oxides such as ITO and IZO; and conductive polymers such as polyaniline, polypyrrole, and polythiophene. These electrode materials may be used alone or in combination. A positive electrode may have a single layer configuration or a multilayer configuration.
A material used for forming a negative electrode has a low work function. Examples of such a material include, but are not limited to, alkali metals such as Li; alkaline-earth metals such as Ca; elemental metals such as Al, Ti, Mn, Ag, Pb, and Cr; alloys of such elemental metals; and metal oxides such as ITO.
In an organic light emitting device according to the present invention, an organic compound layer may be formed by, for example, the following method.
The layer may be formed by vacuum deposition or by a solution application method in which a material is dissolved in an appropriate solvent, the resultant solution is applied to a predetermined position, and the applied solution is dried to remove the solvent.
Hereinafter, applications of an organic light emitting device according to the present invention will be described.
An organic light emitting device according to the present invention may be used for a display apparatus or a lighting apparatus. In addition, such an organic light emitting device may be used for, for example, an exposure light source of an image forming apparatus employing an electrophotographic technique or a backlight of a liquid crystal display apparatus.
A display apparatus includes an organic light emitting device according to the present invention in a display section. The display section includes a plurality of pixels. Such a pixel includes an organic light emitting device according to the present invention and a TFT device. The positive electrode or the negative electrode of the organic light emitting device is connected to the drain electrode or the source electrode of the TFT device. Such a display apparatus may be used as an image display apparatus for a PC or the like.
Alternatively, such a display apparatus may be used for a display section of an image pickup apparatus such as a digital camera or a digital video camera. Such an image pickup apparatus includes a display section and an image pickup section including an image pickup system such as a lens for picking up images. Such a display apparatus may be used not only for a display section of an image pickup apparatus but also for a display section of an inkjet printer.
Such a display apparatus may be an image input apparatus including an image input section configured to receive data from an area CCD, a linear CCD, a memory card, or the like. Such a display apparatus may serve as a display section and an operation panel of an image pickup apparatus or an inkjet printer. That is, the display apparatus may have an image output function of displaying images on the basis of image data input from the outside and an input function of receiving processing data for the images. Such a display apparatus may be used for a display section of a multifunction printer.
Hereinafter, a display apparatus including an organic light emitting device according to the present invention will be described.
Fig. 1 is a schematic sectional view illustrating an organic light emitting device according to the present invention and a TFT device serving as an example of a switching device that is configured to switch between the light-emitting state and non-light-emitting state of the organic light emitting device and is connected to the organic light emitting device. Fig. 1 illustrates two sets of the organic light emitting device and the TFT device. The structure of these devices will be described below in detail.
The display apparatus in Fig. 1 includes a substrate 1 composed of glass or the like and a vapor barrier film 2 that is disposed on the substrate 1 and is configured to protect the TFT devices or an organic compound layer. The display apparatus also includes a gate electrode 3 formed of a metal, a gate insulation film 4, and a semiconductor layer 5.
A TFT device 8 includes the semiconductor layer 5, a drain electrode 6, and a source electrode 7. An insulation film 9 is disposed over the TFT device 8. A positive electrode 11 of an organic EL device is connected to the source electrode 7 through a contact hole 10. Such a configuration is not limitative for a display apparatus and it will suffice that any one of the positive electrode and the negative electrode is connected to any one of the source electrode and the drain electrode of the TFT device.
In Fig. 1, an organic compound layer 12, which is a multilayer organic compound layer, is illustrated as a single layer. A first protective layer 14 and a second protective layer 15 for suppressing degradation of the organic light emitting devices are disposed on a negative electrode 13.
Use of a display apparatus including an organic light emitting device according to the present invention enables displaying of images with stability for a long period of time.
Hereinafter, the present invention will be more specifically described with reference to examples. However, the present invention is not restricted to these examples.
Exemplified compound A1 represented by this formula was synthesized in the following manner. A 100 ml three-neck flask was prepared and charged with 0.40 g (1.46 mmol) of 3-bromofluorene, 0.35 g (14.6 mmol) of lithium amide (product name: lithium amide, manufactured by KISHIDA CHEMICAL Co., Ltd.), 0.49 g (5.0 mmol) of sodium tertiary butoxide (product name: sodium tertiary butoxide, manufactured by TOKYO CHEMICAL INDUSTRY CO., LTD.); further, 20 ml of xylene; while the solution was stirred at room temperature in a nitrogen atmosphere, 0.5 ml (0.15 mmol) of tri-tertiary-butylphosphine (10 wt% hexane solution); and then 0.67 mg (0.153 mmol) of palladium dibenzylideneacetone (product name: palladium dibenzylideneacetone, manufactured by TOKYO CHEMICAL INDUSTRY CO., LTD.). The flask was purged with argon and then the solution in the flask was stirred to reflux for 6 hours. After the reaction was complete, an organic layer was washed with water, dried over anhydrous sodium sulfate, and then purified with a silica gel column (developing solvent mixture of heptane and toluene) to provide 0.14 g (yield: 50.0%) of Exemplified compound A1 (white crystals).
This compound was analyzed by MALDI-TOF MS (matrix assisted ionization time-of-flight mass spectrometry) and M+ of Exemplified compound A1, which is 593.0, was confirmed.
Exemplified compound A1 was subjected to 1H-NMR measurement with an ECA-400 manufactured by JEOL Ltd. (solvent: deuterochloroform) and the delta values (ppm) thereof were found to be 7.56 (2H, dt), 7.42 (1H, dd), 7.32-7.25 (3H, m), 7.10 (1H, dd), and 1.52(6H, s).
The band gap of Exemplified compound A1 was determined from an ultraviolet-visible light absorption spectrum and it was found to be 3.02 eV. In this specification, each band gap was determined with a spectrophotometer U-3010 manufactured by Hitachi, Ltd. from absorption ends of a thin film formed on a glass substrate.
The ionization potential of Exemplified compound A1 was determined with an atmospheric photoelectron spectrometer (measurement apparatus name: AC-1, manufactured by Riken Keiki Co., Ltd.) and it was found to be 5.51 eV.
The Tg of Exemplified compound A1 was measured with a Pyris 1 (manufactured by PerkinElmer, Inc.) and it was found to be 154degree(Celsius). Thus, Exemplified compound A1 had a high thermal stability.
Exemplified compound A1 was further evaluated in terms of amorphousness.
A chloroform solution of Exemplified compound A1 was prepared such that the concentration of Exemplified compound A1 was 0.1 wt%. This solution was dropped onto a glass substrate and spin-coating was performed to form a thin film. After that, the thin film was dried with a vacuum oven at 80degree(Celsius) for 10 minutes to remove the solvent in the thin film.
The resultant substrate was left in the oven at 60degree(Celsius) for a week. Then, the occurrence of crystallization in the film was visually inspected and it was confirmed that no crystallization occurred.
In EXAMPLE 1, by using the following bromo compounds instead of the 3-bromofluorene compound, the following Exemplified compounds can be synthesized.
An organic light emitting device according to the present invention was produced by the following method.
A film of indium-tin oxide (ITO) was formed by a sputtering method on a glass substrate serving as a substrate so as to have a film thickness of 120 nm. Thus, a positive electrode was formed. This positive electrode was subjected to ultrasonic washing with acetone and then isopropyl alcohol (IPA) and then to boiling washing with IPA, and then dried. Furthermore, the positive electrode was subjected to UV and ozone cleaning.
A first hole transport layer was formed on the positive electrode in the following manner. A chloroform solution of Compound 3-1 illustrated below was prepared such that the concentration of Compound 3-1 was 0.1 wt%.
This solution was dropped onto the ITO electrode and spin-coating was performed initially at 500 RPM for 10 seconds and then 1,000 RPM for a minute. After that, the applied solution was dried in a vacuum oven at 80degree(Celsius) for 10 minutes to remove the solvent in the thin film. Thus, the first hole transport layer having a thickness of 11 nm was formed.
Then, a second hole transport layer having a thickness of 20 nm was formed on the first hole transport layer by depositing Exemplified compound A1. In this deposition, film formation conditions used were a degree of vacuum of 1.0 * 10-4 Pa and a film formation rate of 0.1 nm/sec.
A light emitting layer having a thickness of 25 nm was then formed by codepositing Compound 3-3 (illustrated below) serving as a host material and Compound 3-2 (illustrated below) serving as a guest material such that the proportion of Compound 3-3 was 95 wt% and the proportion of Compound 3-2 was 5 wt%.
An electron transport layer having a thickness of 20 nm was then formed by depositing Compound 3-4 illustrated below. A metal layer film having a thickness of 0.5 nm was then formed of a deposition material composed of an aluminum-lithium alloy (concentration of lithium: 1 atom%) on the light emitting layer by a vacuum deposition method. Furthermore, an aluminum film having a thickness of 150 nm was formed by a vacuum deposition method. Thus, an organic light emitting device including the aluminum-lithium alloy film serving as a negative electrode was formed. In the deposition, film formation conditions used were a degree of vacuum of 1.0 * 10-4 Pa and a film formation rate of 1.0 to 1.2 nm/sec.
The thus-formed device was subjected to performance evaluation with a spectroradiometer SR-3 (manufactured by TOPCON CORPORATION). As a result, a blue light emission having a light emission efficiency of 3.23 cd/A and a light emission wavelength of 474.6 nm was observed under the applied voltage of 4.0 V.
When the current density of the device was held at 30 mA/cm2 in a nitrogen atmosphere, the luminance of the device after a lapse of 100 hours was 85% of the initial luminance. Compounds 3-1 to 3-4 are illustrated below.
An organic light emitting device in which a fluorenylamine compound according to the present invention was used as the host material of a light emitting layer was produced.
A film was formed of ITO by a sputtering method so as to have a thickness of 120 nm on a glass substrate serving as a substrate to prepare a positive electrode. This positive electrode was subjected to ultrasonic washing with acetone and then isopropyl alcohol (IPA) and then to boiling washing with IPA, then dried, and then UV and ozone cleaning.
A hole transport layer was formed on the positive electrode in the following manner. A chloroform solution of Compound 3-1 (illustrated above) was prepared such that the concentration of Compound 3-1 was 0.1 wt%.
This solution was dropped onto the ITO electrode and spin-coating was performed initially at 500 RPM for 10 seconds and then 1,000 RPM for a minute. After that, the applied solution was dried in a vacuum oven at 80degree(Celsius) for 10 minutes to remove the solvent in the thin film. Thus, the hole transport layer was formed.
A light emitting layer having a thickness of 25 nm was then formed by codepositing Exemplified compound A1 serving as a host material and Compound 3-2 (illustrated above) serving as a guest material such that the proportion of Exemplified compound A1 was 95 wt% and the proportion of Compound 3-2 was 5 wt%. Furthermore, an electron transport layer and an Al electrode were formed as in EXAMPLE 2.
The thus-formed organic light emitting device was subjected to performance evaluation as in EXAMPLE 2. As a result, a good blue light emission having a light emission efficiency of 2.9 cd/A and a light emission wavelength of 475.0 nm was observed under the applied voltage of 4.0 V.
When the current density of the device was held at 30 mA/cm2 in a nitrogen atmosphere, the luminance of the device after a lapse of 100 hours was 81% of the initial luminance.
In EXAMPLES 1 to 3, the compound in which each of R1 to R6 in the general formula is a methyl group was used. However, when the methyl group is substituted with any one of a hydrogen atom, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group, similar advantages are provided.
This is because such a substituent enhances the degree of amorphousness of the compound without changing the electron state of the compound.
In EXAMPLES 1 to 3, the compound in which each of R21 to R23 in the general formula is a hydrogen atom was used. However, when the hydrogen atom is substituted with any one of a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group, similar advantages are provided. This is because such a substituent enhances the degree of amorphousness of the compound without changing the electron state of the compound.
While the present invention has been described with reference to exemplary embodiments, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. The scope of the following claims is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent structures and functions.
This application claims the benefit of Japanese Patent Application No. 2009-254006, filed November 5, 2009, which is hereby incorporated by reference herein in its entirety.
Claims (9)
- A fluorenylamine compound represented by a general formula below,
the alkyl groups are a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group. - A material for an organic light emitting device, the material being the fluorenylamine compound according to Claim 1.
- An organic light emitting device comprising a pair of electrodes and an organic compound layer disposed between the pair of electrodes, wherein the organic compound layer contains the fluorenylamine compound according to Claim 1.
- The organic light emitting device according to Claim 3, wherein the pair of electrodes are a positive electrode and a negative electrode; the organic compound layer is a hole transport layer; and the hole transport layer is disposed between a light emitting layer and the positive electrode.
- The organic light emitting device according to Claim 3, wherein the organic compound layer is a light emitting layer.
- The organic light emitting device according to Claim 4, wherein the light emitting layer contains a phosphorescence emitting material.
- The organic light emitting device according to Claim 5, wherein the light emitting layer contains a phosphorescence emitting material.
- A display apparatus comprising a plurality of pixels, wherein the plurality of pixels include the organic light emitting device according to Claim 3 and a switching device connected to the organic light emitting device.
- An image input apparatus comprising a display section, an image input section for receiving an image, and a plurality of pixels, wherein the plurality of pixels include the organic light emitting device according to Claim 3 and a switching device connected to the organic light emitting device.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/503,989 US9115055B2 (en) | 2009-11-05 | 2010-10-18 | Fluorenylamine compound, organic light emitting device containing the same, material for organic light emitting device, display apparatus, and image input apparatus |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009254006A JP5578832B2 (en) | 2009-11-05 | 2009-11-05 | Novel fluorenylamine compound and organic light emitting device having the same |
| JP2009-254006 | 2009-11-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2011055493A1 true WO2011055493A1 (en) | 2011-05-12 |
Family
ID=43969737
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2010/006153 WO2011055493A1 (en) | 2009-11-05 | 2010-10-18 | Novel fluorenylamine compound, organic light emitting device containing the same, material for organic light emitting device, display apparatus, and image input apparatus |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US9115055B2 (en) |
| JP (1) | JP5578832B2 (en) |
| WO (1) | WO2011055493A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014015935A2 (en) | 2012-07-23 | 2014-01-30 | Merck Patent Gmbh | Compounds and organic electronic devices |
| EP3345984A1 (en) | 2013-12-06 | 2018-07-11 | Merck Patent GmbH | Connections and organic electronic devices |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10014477B2 (en) | 2012-08-31 | 2018-07-03 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescent element using same |
| KR101684979B1 (en) | 2012-12-31 | 2016-12-09 | 제일모직 주식회사 | Organic optoelectronic device and display including the same |
| KR102639784B1 (en) | 2016-10-25 | 2024-02-26 | 삼성디스플레이 주식회사 | Monoamine compound and organic electroluminescence device including the same |
| CN114068824B (en) * | 2020-07-29 | 2024-04-26 | 江苏三月科技股份有限公司 | Organic electroluminescent device with multi-hole transmission channel material |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0378756A (en) * | 1989-08-23 | 1991-04-03 | Canon Inc | Electrophotographic sensitive body |
| JPH11184109A (en) * | 1997-12-19 | 1999-07-09 | Canon Inc | Electrophotographic photoreceptor and process cartridge having same and electrophotographic apparatus |
| JP2007311759A (en) * | 2006-04-20 | 2007-11-29 | Canon Inc | Organic light emitting device |
| JP2008297535A (en) * | 2006-08-04 | 2008-12-11 | Canon Inc | ORGANIC LUMINESCENT ELEMENT AND BENZO[k]FLUORANTHENE COMPOUND |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6998487B2 (en) * | 2001-04-27 | 2006-02-14 | Lg Chem, Ltd. | Double-spiro organic compounds and organic electroluminescent devices using the same |
| JP4464070B2 (en) * | 2003-05-15 | 2010-05-19 | 出光興産株式会社 | Arylamine compound and organic electroluminescence device using the same |
| US20050123790A1 (en) * | 2003-12-05 | 2005-06-09 | Royster Tommie L.Jr. | Organic element for electroluminescent devices |
| JP5268247B2 (en) * | 2005-12-20 | 2013-08-21 | キヤノン株式会社 | 4-aminofluorene compound and organic light-emitting device |
| US7622865B2 (en) * | 2006-06-19 | 2009-11-24 | Seiko Epson Corporation | Light-emitting device, image forming apparatus, display device, and electronic apparatus |
| JP2010015008A (en) * | 2008-07-04 | 2010-01-21 | Samsung Electronics Co Ltd | Video signal processing apparatus, video signal processing method, program and display device |
-
2009
- 2009-11-05 JP JP2009254006A patent/JP5578832B2/en active Active
-
2010
- 2010-10-18 US US13/503,989 patent/US9115055B2/en active Active
- 2010-10-18 WO PCT/JP2010/006153 patent/WO2011055493A1/en active Application Filing
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0378756A (en) * | 1989-08-23 | 1991-04-03 | Canon Inc | Electrophotographic sensitive body |
| JPH11184109A (en) * | 1997-12-19 | 1999-07-09 | Canon Inc | Electrophotographic photoreceptor and process cartridge having same and electrophotographic apparatus |
| JP2007311759A (en) * | 2006-04-20 | 2007-11-29 | Canon Inc | Organic light emitting device |
| JP2008297535A (en) * | 2006-08-04 | 2008-12-11 | Canon Inc | ORGANIC LUMINESCENT ELEMENT AND BENZO[k]FLUORANTHENE COMPOUND |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014015935A2 (en) | 2012-07-23 | 2014-01-30 | Merck Patent Gmbh | Compounds and organic electronic devices |
| DE202013012401U1 (en) | 2012-07-23 | 2016-10-12 | Merck Patent Gmbh | Connections and Organic Electronic Devices |
| EP3424907A2 (en) | 2012-07-23 | 2019-01-09 | Merck Patent GmbH | Connections and organic electronic devices |
| EP3345984A1 (en) | 2013-12-06 | 2018-07-11 | Merck Patent GmbH | Connections and organic electronic devices |
| EP3693437A1 (en) | 2013-12-06 | 2020-08-12 | Merck Patent GmbH | Compounds and organic electronic devices |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2011098903A (en) | 2011-05-19 |
| US20120211742A1 (en) | 2012-08-23 |
| JP5578832B2 (en) | 2014-08-27 |
| US9115055B2 (en) | 2015-08-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5868195B2 (en) | Novel spiro compound and organic light emitting device having the same | |
| KR101359412B1 (en) | Carbazole derivative, Material for light emitting element, Light emitting element, Light emitting device, and Electronic device | |
| TWI582074B (en) | Fluoranthene derivate, light-emitting element material containing the same and light-emitting element | |
| JP4786917B2 (en) | Organometallic complex, luminescent solid, organic EL device and organic EL display | |
| WO2007043354A9 (en) | Spirofluorene derivative, material for light-emitting element, light-emitting element, light-emitting device, and electronic device | |
| KR101720079B1 (en) | Quinoxaline derivative compound and organic electroluminescent device using the same | |
| US9115055B2 (en) | Fluorenylamine compound, organic light emitting device containing the same, material for organic light emitting device, display apparatus, and image input apparatus | |
| US10680184B2 (en) | Organic electroluminescent materials and devices | |
| JP4880450B2 (en) | Organometallic complex, luminescent solid, organic EL device and organic EL display | |
| JP2020026406A (en) | Organic compound, organic light emitter, display device, imaging device, electronic device, luminaire, and movable body | |
| KR101694496B1 (en) | Dibenzothiophene derivative compound and organic electroluminescent device using the same | |
| JP5595082B2 (en) | Novel benzoxazolylcarbazole compound and organic light emitting device having the same | |
| US9601701B2 (en) | Organic compound and organic light-emitting device | |
| US10840459B2 (en) | Organic electroluminescent materials and devices | |
| JP2014086463A (en) | Novel fused polycyclic compound | |
| US11447437B2 (en) | Organic compound and organic light-emitting element | |
| JP5041767B2 (en) | Carbazole derivatives, materials for light-emitting elements, light-emitting elements, light-emitting devices, and electronic devices | |
| JP5721533B2 (en) | Dispirodibenzonaphthacene compound and organic light-emitting device using the same | |
| WO2014024750A1 (en) | Light emitting element material and light emitting element | |
| JP2020045324A (en) | Organic compound, organic light-emitting element, display apparatus, image pickup apparatus, electronic apparatus, and moving object | |
| JP2020033329A (en) | Organic compound, organic light emitting element, display device, imaging device, electronic apparatus, illumination device and mobile body | |
| JP5495606B2 (en) | Novel condensed polycyclic compound and organic light emitting device having the same | |
| US9590183B2 (en) | Organic compound and organic light-emitting device including the same | |
| CN112300127B (en) | Organic compound, organic light emitting diode and organic light emitting display device including the same | |
| KR20210040255A (en) | Organic compound, organic light-emitting element, display apparatus, image pickup apparatus, lighting apparatus, and moving object |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10828055 Country of ref document: EP Kind code of ref document: A1 |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 13503989 Country of ref document: US |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 10828055 Country of ref document: EP Kind code of ref document: A1 |